Aromatic fluoroalkoxylation via direct displacement of a nitro or fluoro

1876. J. Org. Chem. 1985, 50, 1876-1878 was allowed to warm to room temperature and kept at that temperature for 2 h. The solvent was evaporated and t...
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1876

J . Org. Chem. 1985,50, 1876-1878

was allowed to warm to room temperature and kept a t that temperature for 2 h. The solvent was evaporated and the residue washed with ether (2 X 5 mL) to remove excess triphenylphosphine. Crystallization of the residue from the ethyl acetate-ether mixture gave triphenylphosphonium salt 19 or 20 in a yield 80-90%.

[(Phenylcarbonyl)methyl]triphenylphosphonium perchlorate (19): mp 224-225 OC; IR 1680, 1600, 1440, 1090,980 cm-*; 'H NMR (60 MHz, CDC1,) 7.9-7.5 (m, 20 H, 4 C&), 5.4 (m, 2 H, CH2P+). Anal. Calcd for CzsH22C10J? C, 64.94; H, 4.61. Found: C, 64.65; H, 4.60. (Carbomethoxymethy1)triphenylphosphonium perchlorate (20): mp 155-159 "C; IR 1690, 1435,1090, 980 cm-'; 'H NMR (60 MHz, CDC13) 7.9-7.5 (m, 15 H, 3 CsHS),5.2 (m, 2 H, CH2P+),3.9 (s, 3 H, CH30). Anal. Calcd for CzlHzoCIOsP:

C, 58.01; H, 4.64. Found: C, 57.95; H, 4.66.

Registry NO.3,17043-56-0; 4,66-27-3; 5,80-48-8; 6,52936-24-0; 7, 16156-50-6; 8, 3839-35-8; 9, 13001-92-8; 10, 53059-88-4; 11, 52936-33-1; 12, 58426-27-0; 13, 81971-84-8; 14, 95407-64-0; 15, 88504-82-9; 16, 95407-65-1; 17, 95407-66-2; 18, 95407-67-3; 19, 95407-68-4; 20, 39720-64-4; CH31, 74-88-4; C6H131, 638-45-9; CH3CHICH3, 75-30-9; c-C6HllI, 626-62-0; I(CH&I, 629-09-4; CHZIZ, 75-11-6; PhCOCHJ, 4636-16-2; ICHZCOOH, 64-69-7; ICHzCOOCH3, 5199-50-8; C12, 7782-50-5; H,I06, 10450-60-9; NOZBF4,13826-86-3;Br,, 7726-95-6; m-C1C6H4COOOH,937-14-4; PhI(OCOCF3)2, 2712-78-9; PhIOHOTs, 27126-76-7; Bu4NC104, 1923-70-2; Bu,NOMs, 65411-49-6; Bu4NOTs, 7182-86-7;LiClO,, 7791-03-9;BudNOTf, 35895-70-6;Bu~NOSO~F, 88504-81-8;C1207, 12015-53-1;PPh3, 603-35-0.

Aromatic Fluoroalkoxylation via Direct Displacement of a Nitro or Fluoro Group John P. Idoux,* Mark L. Madenwald, Brent S. Garcia, and Der-Lun Chu Department of Chemistry, Lamar University, Beaumont, Texas 77710

John T. Gupton* Department of Chemistry, University of Central Florida, Orlando, Florida 32816 Received December 7, 1984

Nitro- and fluorobenzenes substituted with a range of electron-withdrawing groups readily undergo fluoroalkoxylation via direct displacement of the nitro or fluoro group. A number of compounds, which cannot be usefully prepared by direct displacement of a chloro group and which are otherwise inaccessible, have been synthesized. Yields and reaction conditions are comparable to those reported by other workers for reactions involving strong nucleophiles.

The nucleophilic displacement of a nitro group from a singly activated aromatic substrate has been effectively used with a variety of strong nucleophiles under dipolar aprotic solvent conditions. For example, at room temperature in DMF, Me2S0, or HMPA, hydroxy or alkoxy1 anions,'-, thiol anion^,'^^^^ sulfinate anions,l and oximate anions7effect a synthetically useful displacement of a nitro group from ~arbonyl,'-~,~J nitro,'s7 cyan0,''~9~,~ sulfone,' and aryl7 activated substrates. Each of these procedures are formal, "one-pot" displacements of the nitro group and represent transformations which, in general, occur more readily compared to the corresponding chloro leaving group substrates. Similarly, as we8 and othersg have previously demonstrated, fluoro is comparable to nitro in leaving group ability in an SnAr reaction. In connection with our interest in aromatic fluoroalkoxylation via direct aromatic nucleophilic (1) Kornblum, N.; Cheng, L.; Kerber, R. C.; Kestner, M. M.; Newton, B. N.; Pinnick, H. W.; Smith, R. G.; Wade, P. A. J . Org. Chem. 1976,41, 1560. (2) Gorvin, J. H. Chem. Znd. (London) 1967, 36, 1525. (3) Rodlmann, E.; Schmidt, W.; and Nischk, G. E. Makromol. Chem. 1969, 130, 45. (4) Mauleon, D.; Granados, R.; Minguillon, C. J. Org. Chem. 1983,48, 21 n5

(5) Beck, J. R. J. Org. Chem. 1972, 37, 3224. (6) Beck, J. R. J. Org. Chem. 1973, 38, 4086. (7) Knudsen, R. D.; Snyder, H. R. J. Org. Chem. 1974, 39, 3343. (8)Idoux, J. P.; Gupton, M. T.; McCurry, C. K.; Crews, A. D.; Jurss, C. D.; Colon, C.; Rampi, R. J. Org. Chem. 1983, 48, 3771. (9) March, J. 'Advanced Organic Chemistry", 2nd ed.; McGraw-Hill: New York, 1977. (10) Gupton, J. T.; Idoux, J. P.; Colon, C.; Rampi, R. Synth. Commun. 1982, 12, 695. (11) Gupton, J. T.; Idoux, J. P.; De Crescenzo, G.; Colon, C. Synth. Commun. 1984, 24, 621. 0022-3263/85/1950-1876$01.50/0

we have recently reporteds that certain fluoroalkoxide anions react in dipolar aprotic solvents with activated aryl and heteroaryl chlorides at temperatures of 90-150 OC to produce the corresponding fluoroalkyl ethers. While a number of dipolar aprotic solvent promote the reaction (HMPA, DMF, Me2S0, and l-methyl-2-pyrrolidinone), HMPA provided the most consistent set of reactive conditions. As expected, cyano and nitro groups were particularly effective activators and provided virtually quantitative, isolated yields of ortho- and para-substituted products with 2,2,2-trifluoroethoxide ion as the nucleophile and extremely good (-80%) yields of the corresponding meta-substituted products. The trifluoromethyl, phenylcarbonyl, and phenylsulfonyl groups proved to be sufficiently activating so as to provide modest to fair yields (30-60 % ) of the corresponding (2,2,2-trifluoroethoxy)benzenes; however, chloro-, aldehydo-, carbomethoxy-,and amido-substituted chlorobenzenes provided either no reaction or only traces of product. Additionally, with 4chlorobenzonitrile as substrate, tertiary fluoroakoxide ions (e.g., -OC(CH3)&F3)and fluoroalkoxide ions containing more than four fluorines promote little, if any, direct fluoroalkoxylation; even the four fluorine nucleophile -OCH2CF2CF2Hgave only a modest yield (-40%) of fluoroalkoxylated product when reacted with 4-chlorobenzonitrile at 200 "C. Because of our interest in extending the general synthetic usefulness of direct aromatic nucleophilic fluoroalkoxylation, we felt it would be of value to examine the reaction of a set of substrates containing a potentially more reactive leaving group than chloro. Thus, a range of monosubstituted nitrobenzenes or fluorobenzenes have been investigated. 0 1985 American Chemical Society

J. Org. Chem., Vol. 50, No. 11, 1985 1877

Aromatic Fluoroalkoxylation

Results and Discussion

Table I. Reaction of Substituted Nitro- and Fluorobenzenes with NaOCH2CF3"

As indicated in Table I, a wide range of monosubstituted nitro- and fluorobenzenes undergo a synthetically useful reaction with the 2,2,2-trifluoroethoxide ion a t or near room temperature. It should be emphasized that the reported yields refer to pure, isolated products and, in all cases, represent better yields and milder conditions than those reported previously8.1° when the corresponding monosubstituted chlorobenzenes were used as substrates. For example, cyano (la-d), nitro (le-f), trifluoromethyl (lg), phenylsulfonyl (lh,i),and phenylcarbonyl (1j) activated nitro- and fluorobenzenes gave markedly improved yields of the trifluoroethoxy product at reaction temperatures of 25-50 "C compared to 150 "C for reaction of the corresponding substituted chlorobenzenes. While the reaction time as noted in Table I is 15-18 h, a time study of la indicated that the reaction was essentially complete within 1.5 h. Of particular interest is the fact that the carbomethoxy (lk),aldehydo (11-lo), methylcarbonyl (lp-lr), and amido (1s-lu) functionalities are sufficiently activating in nitroor fluorobenzenes so as to provide synthetically useful processes a t 25 "C; in contrast, the corresponding chlorobenzenes gave no reaction a t 150 "C. In the case of the aldehydo (11-lm) and methylcarbonyl (lp-lq) substituted nitrobenzenes, a significant exotherm (-80 "C) occurs when the reaction is initiated a t 25 "C due apparently to the nitro group's ability to activate the carbonyl groups toward a Cannizzaro or condensation reaction, respectively. For the correspondingly substituted fluorobenzenes (lnlo, lr) only a mild exotherm (-10 "C) is observed and the yields of the desired fluoroalkoxylated materials are substantially improved. Even o-difluorobenzene (lw) undergoes a smooth, monofluoroalkoxylation (at 90 "C), whereas o-dichlorobenzene gave only a trace (NMR) of product at 150 "C. At a higher temperature (lx, 120 "C) the yield of the monofluoroalkoxylated material is substantially improved but, interestingly, difluoroalkoxylation occurs as well to give a product mixture composed of approximately 4.5/ 1 mono-/disubstituted products (see 2x in Experimental Section). While not synthetically useful, the parent compounds, nitrobenzene (lz) and fluorobenzene (laa),do give traces (NMR) of product at 90 "C and 120 "C, respectively. Finally, it is interesting to note that the presence of an ortho electron-donating group in a sufficiently activated molecule (lv) has little affect on the reaction. Because our previous investigations8 indicated that a variety of other fluoroalkoxide ions were relatively unreactive toward 4-chlorobenzonitrile, we have subjected a more reactive substrate (4-nitrobenzonitrile) to the same set of fluoroalkoxide ions. As indicated in Table 11, all of the various fluoroalkoxide ions, with the exception of OCH(CF3),, undergo synthetically useful reactions with 4-nitrobenzonitrile; in contrast, only product 3d could be usefully obtained via reaction with 4-chlorobenzonitrile as substrate and then only under considerably more severe conditions. In conclusion, the direct fluoroalkoxylation of substituted nitro- and fluorobenzenes provides a wide variety of otherwise inaccessible, substituted fluoroalkoxylated materials. This simple and efficient synthetic entry to fluoroalkoxy aromatics could be particularly useful in relation to the many important uses of fluorinated materia1s.12~13 (12) Gerstenberger, M.; Haas, A. Angew. Chem., Int. Ed. Engl. 1981, 20, 647. (13)Chem. Eng. News 1984,Sept 10, 32.

XPhY

----

XPhOCH,CF,

1

substrate la lb IC

Id le If 1g lh li Ij

lk 11 lm In lo 1P

1q lr 1s It lu lv

lw lx 1Y 12 1aa

lbb

2

X 4-CN 4-CN 4-CN 3-CN %NO2

Y

2-CF3 4-(4-FPhS02) 4-(4-FPhS02) 4-COPh 4-COOMe 4-CHO 4-CHO 4-CHO 4-CHO 4-COMe 4-COMe 4-COMe 4-CONMe2 4-CONEt2 4-SOZNEt2 4-NO2,2-Me 2-F 2-OCH2CF3 2-Ph H H 2-OEt

yield of 2,* % 95 (64) 85' 58d 84d (57) 78 93 68 (32)' 9lf (60) 998 (69) 70 (54) 73 (nr) 24hfi(nr) 37hJ 44k 56' lom (nr) 1On

86k 65 (nr) 64 79 89 15" (trace)Pjq 39' traceq traceq@ trace**' nrf

"Unless otherwise noted, all reactions were run in HMPA at 25 "C for 18-20 h. *Yields refer to isolated, purified (distillation or recrystallization) materials and were found to be greater than 90% pure by TLC. The values in parentheses refer to yields reported in ref 8 or 10 for the corresponding product from substrates with Y = C1. Reaction run in DMF. Reaction run at 50 "C. e Yield is for the 4-CF, isomer. fReaction was run with 1 equiv of NaOCH,CF, to give the monosubstituted product. Reaction was initiated and run at 0-10 "C for 2-3 h and then allowed to come to room temperature. BReaction was run with 2 equiv of NaOCH2CF3to give the disubstituted product. Reaction was initiated and run at 0-10 "C for 2-3 h and then allowed to come to room temperature. hReaction was initiated and run at 0-10 "C for 2-3 h and then allowed to come to room temperature. If reaction is initiated at 25 "C, a significant exotherm (70-75 "C) occurs and the isolated yield of fluoroalkoxylated material is diminished. 'Workup involved dilution with water. j Workup involved dilution with aqueous saturated sodium chloride. Reaction was initiated and run at 0-10 "C for 2-3 h and then allowed to come to room temperature. 'Reaction was initiated and run at 0-10 "C for 2-3 h, allowed to come to room temperature, and then heated at 90 "C for 12 h. Reaction was initiated at 25 "C accompanied by a rapid, significant exotherm (80-90 "C). "Reaction was initiated at 0 "C by slow, dropwise mixing and was accompanied by exotherming (10-15 "C). "Reaction was run a t 90 "C. PSubstrate was o-dichlorobenzene. Reaction was run at 150 "C. "Determined by NMR analysis of the crude reaction mixture. Reaction was run at 120 "C. Product mixture contained compound 2w and o-bis(2,2,2-trifluoroethoxy)benzene in a 4.5/1 ratio, respectively. Reaction was run at 90 "C. Reaction was run at 120 "C.

Experimental Section14 The procedure reported previouslys is typical of the experimental conditions used for reaction of substituted nitro- and (14)Infrared spectra were recorded on a Perkin-Elmer Model 710B infrared spectrometer. NMR spectra were obtained neat or in CC4, CDCl,, or Me2SO-d6solutions vs. (CH,),Si as internal standa -1 at 90 MHz with a Varian EM390 spectrometer. The GC/MS of 2g dnd 2s were obtained on a Hewlett Packard 5890A gas chromatography/HP597OB mass selective detector system. Combustion analyses were carried out by Robertson Laboratory, Inc., Florham Park, NJ. All boiling points and melting points are uncorrected and melting points were recorded on a Thomas-Hoover capillary melting point apparatus.

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J. Org. Chem., Vol. 50, No. 11, 1985

Idoux e t al.

Table 11. Reaction of 4-Nitrobenzonitrilewith Various Sodium Fluoroalkoxides (NaORF)" 02NPhCN-4

-

RPPhCN-4

3

product 3a 3b

3c 3d 3e

3f 3g

Rp or ORF CHZCF3 CHZCFzCF3 CH(CH3)CFB CH(CHJCF3 C(CHJzCF3 CHZCF2CF2CF3 CH(CF3h

reactn temp, "C 25 150 25 90 25 150 150

yield of 3,b% 95 (64) 55 (nr) 51 (nr) 78 (72, crude) 62 (nr) 5OC(nr) nr (nr)

"All reactions were run in HMPA for 18-20 h. bYields refer to isolated, purified (distillation or recrystallization) materials and were found to be greater than 90% pure by TLC. The values in parentheses refer to yields reported in ref 8 for the corresponding product from reaction at 150 "C with 4-chlorobenzonitrile as substrate. Product mixture contained compound 3f and 4-cyano-N,N-dimethylaniline15in an approximately 1/1 ratio (NMR). fluorobenzenes. The only changes are those noted in Tables I and I1 for reaction time and temperature and the substitution of a saturated aqueous sodium chloride solution for the 5% aq hydrochloric acid in the workup. The spectra and physical property data for compounds 2a-f, 2h-j, and 3c,d were in agreement with those reported previously.8JO 2-(2,2,2-Trifluoroethoxy)benzotrifluoride(2g): bp 50-51 "C (0.5 mm); NMR (neat) 6 4.28 (q, J = 8 Hz, 2 H), 6.81-7.13 (m, 2 H), 7.33-7.60 (m, 2 H); IR (thin film) 1620,1600,1505,1470, 1340,1170,980,870,840,765cm-', mass spectrum, m l e 244.15 (M+). Methyl 4- (2,2,2-Trifluoroethoxy)benzoate (2k): mp 53-55 "C; NMR (CDC1,) 6 3.83 ( 8 , 3 H), 4.35 (4,J = 8 Hz, 2 H), 6.93 (d, J = 8 Hz, 2 H), 8.00 (d, J = 8 Hz, 2 H); IR (CCld) 1720,1610, 1290, 1250, 1180, 1120, 1080, 860 cm-'. Anal. Calcd for c1&$303: C, 51.28 H, 3.85. Found C, 51.64; H , 3.63. 4-(2,2,2-Trifluoroethoxy)benzaldehyde (2n): bp 82-85 "C (0.3 mm); NMR (CDCl,) 6 4.40 (q, J = 8 Hz, 2 H), 6.98 (d, J = 8 Hz, 2 H), 7.75 (d, J = 8 Hz, 2 H), 9.81 (s, 1 H); IR (thin film) 1680, 1590, 1495, 1280, 1240, 1160, 1070, 970, 870, 830 cm-'. Anal. Calcd for C4H7F302: C, 52.94; H, 3.43. Found C, 52.90; H, 3.42. 4-(2,2,2-Trifluoroethoxy)acetophenone (2r): mp 70-72 "C; NMR (CDC1,) 6 2.53 (s, 3 H), 4.33 (q, J = 8 Hz, 2 H), 6.89 (d, J = 8 Hz, 2 H), 7.85 (d, 8 Hz, 2 H); IR (CHCl,) 1670,1590,1500, 1410, 1350, 1280, 1230, 1160, 1060, 960, 860, 830 cm-'. Anal. Calcd for Cl,&F302: C, 55.05; H, 4.13. Found C, 54.74; H, 4.06.

3400, 1620, 1580, 1290, 1160, 1070, 840, 820 cm-'. And Calcd for CllH12F3N02:C, 53.44; H, 4.86; N, 5.67. Found: C, 53.55; H, 4.57; N,5.35. 4-(2,2,2-Trifluoroethoxy)-NJV-diethylbenzamide(2t): mp 57-59 "C; NMR (CDC1,) 6 1.16 (t,6 Hz, 6 H), 3.35 (4, 6 Hz, 4 H), 4.32 (q, 8 Hz, 2 H), 6.92 (d, 8 Hz, 2 H), 7.33 (d, 8 Hz, 2 H); IR (CHC1,) 3450, 1620, 1580, 1295, 1170, 1080, 845 cm-'.

4-(2,2,2-Trifluoroethoxy)-N,N-diethylbenzenesulfonamide (2u): mp 70-73 "C; NMR (CDCl,) 6 1.16 (t, 6 Hz, 6 H), 3.22 (4, 6 Hz, 4 H), 4.40 (q,8 Hz, 2 H), 7.00 (d, 8 Hz, 2 H), 7.77 (d, 8 Hz, 2 H); IR (CHCl,) 1600, 1300, 1340, 1260, 1170, 840, 810 cm-'. Anal. Calcd for Cl2Hl6F3NO3S: C, 46.30; H, 5.14; N, 4.50. Found: C, 46.39; H, 5.27; N, 4.32. 2-(2,2,2-Trifluoroethoxy)-4-nitrotoluene (2v): mp 50-51 "C; NMR (CC14)6 2.31 ( 8 , 3 H), 4.41 (q, J = 8 Hz, 2 H), 6.81 (d, J = 10 Hz, 1H),7.98 (m, 2 H); IR (CHCl,) 3020,1600,1520,1460, 1360, 1300, 1260, 1220, 1180, 1110, 1080, 990, 940 cm-'. Anal. Calcd for CJ-18F3N03: C, 45.96; H, 3.40; N, 5.96. Found: C, 45.98; H, 3.45; N,5.74. 2-(2,2,2-Trifluoroethoxy)fluorobenzene(2w): bp 40 "C (1 mm); NMR (neat) 6 4.22 (q, J = 8 Hz, 2 H), 6.89 (m, 4 H); IR (thin film) 3060,2950,2880,1610,1600,1500,1460,1420,1300, 1200, 1120, 1070, 1040, 980, 970, 870, 850, 790, 760 cm-'. Anal. Calcd for C8H6F40: c, 49.48; H, 3.09. Found c, 49.28; H, 3.02.

Mixture of 2-(2,2,2-Trifluoroethoxy)fluorobenzene and o-Bis(2,2,2-trifluoroethoxy)ben~ene (2x): bp 63-70 "C (3 mm); NMR (CC14) 6 4.22 (4,J = 8 Hz), 4.19 (q, J = 8 Hz) GC/MS, fraction at 1.752 min, m f e 194.05 (M'), fraction at 3.833 min, mle 274.00 (M+). 4-(2,2,3,3,3-Pentafluoropropoxy)benzonitrile(3b): bp 8U-85 "C (0.2 mm); NMR (CDC1,) 6 4.45 (t, J = 10 Hz, 2 H) 6.98 (d, J = 8 Hz, 2 H), 7.56 (d, J = 8 Hz, 2 H); IR (thin film) 2220,1600, 1570,1500,1450,1370,1295,1260,1170,1150,1100,1065,1020, 940, 840 cm-'. Anal. Calcd for ClJ16F5NO: C, 47.81; H, 2.39; N, 5.58. Found: C, 48.18; H, 2.46; N, 5.74. 4-(2,2,2-Trifluoro-tert-butoxy)benzonitrile (3e): bp 82-86 "C (0.15 mm); NMR (CDCl,) 6 1.48 (s, 6 H), 7.01 (d, J = 8 Hz, 2 H), 7.51 (d, J = 8 Hz, 2 H); IR (thin film) 2220,1590,1490,1460, 1390, 1320, 1220, 1170, 1125, 1010, 960, 890, 860 cm-'. Anal. Calcd for Cl1Hl$,NO: C, 57.64; H, 4.37; N, 6.11. Found C, 57.80; H, 4.35; N, 6.38.

Mixture of 4-(2,2,3,3,4,4,4-Heptafluorobutoxy)benzonitrile and 4-Cyano-N,N-dimethylaniline (3f): bp 105-110 "C (0.3 mm); NMR (CDCl,, dimeth~laniline),'~ 6 3.00 (s, 6 H), 6.55 (d,

J = 8 Hz, 2 H), 7.32 (d, J = 8 Hz, 2 H); benzonitrile 6 4.45 (t, J = 10 Hz, 2 H), 6.93 (d, J = 8 Hz, 2 H), 7.52 (d, J = 8 Hz, 2 H).

Acknowledgment. We a r e grateful t o t h e Petroleum Research Fund, administered b y the American Chemical Society. for partial s u p p o r t of t h i s work.

4-(2,2,2-Trifluoroethoxy)-N,N-dimethylbenzamide (2s): mp 94-96 "C; NMR (Me2SO) 6 2.90 ( s , 6 H), 4.72 (4, J = 8 Hz, 2 H), 7.01 (d, J = 8 Hz, 2 H), 7.36 (d, J = 8 Hz, 2 H); IR (nujol)

(15) Gupton, J. T.; Idoux, J. P.; Baker, G.; Colon, C.; Crews, A. D.; Jurss, C. D.; Rampi, R. J. Org. Chen. 1983, 48, 2933.